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HRID 1741865作成日:2026年10月26日

Thiophene-3-carboxylic acid → 4-Ethyl-2-propyl-1-(3-thenoyl) semicarbazide

https://huagongshe.com/reaction/1741865

反応式

関与物質

役割名称HCID仕込み量
反応物Thiophene-3-carboxylic acidHCID 6918—
反応物TriethylamineHCID 8471—
反応物Isobutyl chloroformateHCID 62365—
反応物4-Ethyl-2-propyl semicarbazideHCID 19010929—
溶媒TetrahydrofuranHCID 8028—
生成物4-Ethyl-2-propyl-1-(3-thenoyl) semicarbazideHCID 54099638—

反応条件

温度5 °C

反応手順

A stirred solution of 2.62 g (20.5 mmol) of thiophene-3-carboxylic acid and 2.8 mL (20.0 mmol) of triethylamine in 20 mL of THF was cooled to 5° C. and 2.6 mL (20.0 mmol) of isobutyl chloroformate was added dropwise over 5 minutes. The mixture was stirred at 5° C. for 5 minutes and added to a suspension of the 4-ethyl-2-propyl semicarbazide prepared above in 20 mL of THF at 5° C. This mixture was allowed to warm to room temperature and stirred overnight. The mixture was concentrated to remove most of the solvent, taken up in 75 mL of water and extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate extracts were washed with 50 mL of 5% aqueous HCl and 50 mL of saturated aqueous sodium bicarbonate (NaHCO3), and dried over MgSO4. Removal of the solvent left 5.30 g of crude 4 -ethyl-2-propyl-1-(3-thenoyl) semicarbazide as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05334726
出典データセットuspto-grants-1994_08
ORD IDord-3788da22400547588000d5e5ed67015c
出典メモuspto-grants-1994_08